IRCT2017082935979N1已完成2 期
Comparing the analgesic effect of intrathecal Sufentanil with intravenous Acetaminophen in combination with low-dose ketamine onl abor pain
Vice chancellor for research in Qazvin university of medical sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- no limit 至 no limit(—)
- 性别
- Female
入选标准
- •Inclusion criteria are as follows:
- •oPregnant women who are candidates for natural delivery and are in the active phase (Cervical dilatation of 5-3 cm);
- •oPregnant women with no history of physical and psychological illness or biochemical abnormalities (ASA I class);
- •oPregnant women who have written and complete consent for the study.
- •Exclusion criteria are as follows:
- •oDissatisfaction pregnant women;
- •oMother's preeclampsia and eclampsia;
- •oInsulin-dependent diabetes;
- •oMother drug abuse history;
- •oUsing any analgesic method before entering the study;
- •oHistory of liver disease;
- •oHistory or presence of bleeding disorder and coagulation disorders in the mother;
- •ousing anticoagulant drugs;
- •oHistory of mental illness or using antidepressants or anticonvulsants;
- •oAny contraindication for spinal anesthesia;
- •oHistory of allergic reactions or intolerant to the drugs studied (Sufentanil, acetaminophen and ketamine);
- •oAny significant or severe systemic disease that limits usual and natural activities (such as kidney disease that require dialysis, class 2 heart failure and ….).
排除标准
- 未提供
研究者
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